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Fedovapagon (VA106483) is a selective and potent agonist of the vasopressin V2 receptor (V2R) that inhibits the growth of intersegmental vessels in zebrafish. It can be used to study overactive bladder, nocturia, and painful bladder syndromes.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
5 mg | $113 | In Stock | |
10 mg | $179 | In Stock | |
25 mg | $392 | In Stock | |
50 mg | $689 | In Stock | |
100 mg | $973 | In Stock | |
1 mL x 10 mM (in DMSO) | $126 | In Stock |
Description | Fedovapagon (VA106483) is a selective and potent agonist of the vasopressin V2 receptor (V2R) that inhibits the growth of intersegmental vessels in zebrafish. It can be used to study overactive bladder, nocturia, and painful bladder syndromes. |
Targets&IC50 | V2R:24 nM (EC50) |
In vivo | In rats, oral administration of fedovapagon at a dose of 1 mg/kg results in an 81% inhibition rate of urine output[1]. |
Alias | VA483, A106483 |
Molecular Weight | 462.58 |
Formula | C27H34N4O3 |
Cas No. | 347887-36-9 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
Solubility Information | DMSO: 50 mg/mL (108.08 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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